Search the 36 jobs at PSI CRO

The Site Identification Specialist is responsible for site identification and new clinical trial placement, creating a site identification tracker, developing a site database, and training CTAs and CRAs. They communicate with project teams to provide updates and assist with enrollment by identifying additional sites, utilizing external databases, and participating in client presentations.

As an IT Systems Engineer, you will maintain and improve IT infrastructure systems, design new computer systems, manage networks, and implement maintenance procedures. You will also troubleshoot errors, optimize backup processes, and document technical specifications while delivering training on IT systems.

As an IT Systems Administrator, you will provide daily technical support, troubleshoot desktop systems and peripherals, perform installations and upgrades, assist with data management and inventory, and support users in the Asia Pacific region.

The Site Management Associate will support clinical research projects by maintaining databases, managing documents, serving as a contact point for vendors, coordinating communication with investigative sites, and assisting with administrative tasks related to project meetings and payments.

The Referral Specialist will build and manage a referral network, implement referral processes, train referring physicians, conduct qualification visits, and maintain documentation related to referrals. The role requires effective communication with physicians and the ability to work independently and as a part of a team.

In this role, you will evaluate, test, and implement IT infrastructure systems to support business processes. You will maintain, upgrade, and improve IT systems and networks, manage configurations, troubleshoot issues, optimize processes, and deliver training on IT system procedures.

The IT Systems Engineer will maintain and improve IT infrastructure systems and networks, designing new frameworks, managing configurations, troubleshooting errors, and optimizing processes including backup/restore. Responsibilities include handling server and network hardware, creating guidelines and manuals, delivering training, and supporting various IT solutions within a collaborative team environment.

The Office Manager ensures smooth day-to-day office activities, coordinates local administrators, manages office suppliers and services, supports HR processes, organizes meetings and events, prepares administrative reports, and oversees logistics for employee relocation.

The Administrator in Office Management assists with ordering and inventory of office supplies, handles maintenance of office equipment, manages office meetings, and deals with incoming correspondence. This role involves secretarial support, maintaining reports, and ensuring office security by controlling access.

The Lead Data Manager oversees data management activities for clinical projects, ensuring quality data entry, coordination of data validation, and communication with project teams and vendors. Responsibilities include developing data management plans, conducting database locks, and training team members in clinical data management.

As a SAS Programmer I, you will contribute to statistical programming for global clinical trials, developing datasets and programming requirements. You will support validations of SAS programs, prepare documentation, and collaborate with project teams in clinical research.

The SAS Programmer I will work on statistical programming for global clinical trials, developing analysis data sets, programming requirements, SAS ADS, and TFLs while supporting program validations and collaborating with project teams.

As a Full Stack Developer at PSI, you will architect, develop, and maintain web-based applications for internal clients, process user requests, prepare documentation, perform software testing, and participate in code reviews while adhering to development standards.

As an Associate Legal Counsel, you will provide legal support focused on local matters in Ukraine, including reviewing and drafting contracts, providing legal advice, and ensuring compliance with company policies. You will collaborate closely with various departments and assist in legal matters related to clinical trials.

As a Budget Specialist, you will support clinical research projects by reviewing and negotiating site budgets, facilitating agreements, and maintaining documentation. You'll work with various teams to ensure contracts are executed and tracked, contributing to the efficient functioning of clinical trials.

As a Full Stack Developer at PSI, you will develop and maintain business applications, process user requests, prepare documentation, implement software tests, and track development tasks. You will also remain updated on systems development technologies.

As a Full Stack Developer, you'll architect, develop, and maintain business applications, support internal IT system requests, document development processes, conduct code reviews and testing, and adhere to development standards. The position requires collaboration and staying updated with technological advancements.

The Site Management Associate I supports clinical research projects by managing communication, documents, and site-related tasks. Responsibilities include query resolution, ensuring compliance with local regulations, coordinating audits, and managing supplies and training for site teams.

As a Site Management Associate I, you will support clinical research projects by managing communications, maintaining systems, handling document management, and ensuring compliance with regulations. You will act as a liaison for site personnel and oversee the inventory of clinical supplies, regulatory submissions, and training for project teams, facilitating efficient project execution.

The Site Management Associate I will support clinical research projects by managing communication, coordinating site activities, and handling documents while ensuring compliance with regulatory standards. Responsibilities include acting as a liaison between site personnel and clinical research associates, managing supplies, tracking regulatory submissions, and overseeing audit preparations.